Clinical Research Associate (CRA II/Senior) - West (Ophthalmology)
Company: Parexel International Corporation
Location: Billerica
Posted on: October 23, 2024
Job Description:
Working with heartAt the end of the day we're all patients.
Because of this, the Parexel team takes our work personally and
does it with empathy and heart. When our values align, there's no
limit to what we can achieve. Our clinical operating model drives
effectiveness, reduces handoffs and increases employee, client and
site satisfaction. As a Clinical Research Associate at Parexel, you
will be joining a team with a wide variety of experiences and
knowledge. We hire talent that takes initiative to do things
better, smarter and faster- people who want to grow personally and
professionally.Your time here At Parexel, the CRA role offers the
opportunity to go beyond the role of a typical clinical monitor.
CRA's are accountable for using their expertise to build and
maintain the site relationship and ensure they are set up for
success. As the clinical sites' sole point of contact, this
includes addressing and resolving site issues and questions. You
will also manage site quality and delivery from site identification
through to close-out.As a CRA, Parexel will offer you world class
technology and training catered to your individual experience. You
can anticipate less travel and a lower protocol load in comparison
to industry peers. Your hard work may be rewarded through a bonus
incentive program, the opportunity to work within multiple
therapeutic areas and an opportunity to advance your career in
clinical research. If impact, flexibility, and career development
appeal to you, Parexel may be your next home.What you'll do
- Leverage your expertise. Conduct qualification visits (QV),
site initiation visits (SIV), monitoring visits (MV) and
termination visits (TV) at assigned clinical sites and generate
visit/contact reports.
- Build relationships. Oversee integrity of the study and utilize
problem-solving skills to promote rapport with the site and
staff.
- Protect patients. Review the performance of the trial at
designated sites, ensure the rights and well-being of human
subjects are safeguarded and are in accordance with protocol.
- Drive productivity. Develop patient recruitment strategies in
conjunction with the clinical site to meet enrollment timelines
while also Ensuring compliance with the approved standard operating
procedures (SOPs), protocol/amendment(s), GCP, and the applicable
regulatory requirement(s).
- Ensure quality. Evaluate the quality and integrity of the
reported data, site efficacy and drug accountability.
- Execute. Monitor completeness and quality of Regulatory
Documentation and perform site document verification.A little about
usParexel is proud to be a leading Clinical Research Organization
with team members across the globe. As a member of our team, you
will get to know your colleagues on a personal level. Have a
question? A clinical research leader, project team member,
technology "super user" or colleague are a phone call away. Our
clinical research teams meet regularly to have discussions in an
open environment, allowing our team members to share their
expertise and promote learning within the team. Management supports
and encourages career growth through consistent performance
discussions and evaluations. Whether your interest is to progress
into a more senior level CRA role, into line management, Quality,
Project Leadership or a variety of other positions, Parexel prides
itself on career opportunities for our employees.More about youOn
your first day we'll expect you to have:
- 18+ months Clinical Research Associate (CRA) monitoring
experience in clinical research with understanding of clinical
trials methodology and terminology.
- Bachelors or equivalent degree in biological science, pharmacy
or other health related discipline.
- Strong interpersonal, written, and verbal communication skills
within a matrixed team.
- Ability to work in a self-driven capacity with a sense of
urgency and limited need for oversight.
- A client focused approach to work with a flexible attitude with
respect to assignments and new learning.
- The ability to manage multiple tasks, evaluate a variety of
unpredictable scenarios and achieve project timelines while being
able to apply your understanding of study protocol(s).
- An honest and ethical work approach to promote the development
of life changing treatments for patients.
- Oncology/ophthalmology experience preferred.
- Strong computer skills, including but not limited to the
knowledge of a Clinical Trial Management System (CTMS), Electronic
Document Management System (EDMS) and MS-Office products such as
Excel and Word.#LI-REMOTE
Keywords: Parexel International Corporation, Billerica , Clinical Research Associate (CRA II/Senior) - West (Ophthalmology), Healthcare , Billerica, Massachusetts
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